Catalytic enantioselective access to N(III)-stereogenic aziridines via chiral brønsted acid-catalyzed N-Cl bond formation.

Zheng Y, Liao M, Hao GF, Jin LH, Jayawardana BC, Marambe B, Xiong Q, Wu X

Open source

DOI
10.1039/d6cc02512a
Published
2026 Jul 7
Container
Chemical communications (Cambridge, England)
Publisher
Not recorded
Open access
unknown

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BibTeX

@article{allodium:10.1039/d6cc02512a,
  title = {Catalytic enantioselective access to N(III)-stereogenic aziridines via chiral brønsted acid-catalyzed N-Cl bond formation.},
  author = {Zheng Y and Liao M and Hao GF and Jin LH and Jayawardana BC and Marambe B and Xiong Q and Wu X},
  year = {2026},
  journal = {Chemical communications (Cambridge, England)},
  doi = {10.1039/d6cc02512a},
  url = {https://doi.org/10.1039/d6cc02512a}
}

RIS

TY  - JOUR
TI  - Catalytic enantioselective access to N(III)-stereogenic aziridines via chiral brønsted acid-catalyzed N-Cl bond formation.
AU  - Zheng Y
AU  - Liao M
AU  - Hao GF
AU  - Jin LH
AU  - Jayawardana BC
AU  - Marambe B
AU  - Xiong Q
AU  - Wu X
PY  - 2026
JO  - Chemical communications (Cambridge, England)
DO  - 10.1039/d6cc02512a
UR  - https://doi.org/10.1039/d6cc02512a
ER  - 

APA

Y, Z., M, L., GF, H., LH, J., BC, J., B, M., Q, X., & X, W. (2026). Catalytic enantioselective access to N(III)-stereogenic aziridines via chiral brønsted acid-catalyzed N-Cl bond formation.. Chemical communications (Cambridge, England). https://doi.org/10.1039/d6cc02512a

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